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rs397509322

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509322(A;A)
Make rs397509322(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094740
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509322
ebirs397509322
HLIrs397509322
Exacrs397509322
Varsomers397509322
Maprs397509322
PheGenIrs397509322
hapmaprs397509322
1000 genomesrs397509322
hgdprs397509322
ensemblrs397509322
gopubmedrs397509322
geneviewrs397509322
scholarrs397509322
googlers397509322
pharmgkbrs397509322
gwascentralrs397509322
openSNPrs397509322
23andMers397509322
23andMe allrs397509322
SNP Nexus

SNPshotrs397509322
SNPdbers397509322
MSV3drs397509322
GWAS Ctlgrs397509322
Max Magnitude0
ClinVar
Risk rs397509322(A;A)
Alt rs397509322(A;A)
Reference rs397509322(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246757C>T
CLNSRC ClinVar
CLNACC RCV000049136.2,